Compactcath, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2018-06-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K180738 | COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter | EZD | 2018-06-14 | View |
| 510(k) | K160858 | CompactCath Intermittent Urinary Catheter | EZD | 2016-04-26 | View |
No matching devices.